Neudle.com: "amyotrophic lateral sclerosis natural history"

Differential
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acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

advance directives

advances in neurology

algorithm

Alzheimer's disease

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

analgesic

anterior horn cell disease

aphasia, progressive, primary

asthma, poliomyelitis-like syndrome with

bulbar palsy, progressive

cachexia

camptocormia

cane

carbon monoxide poisoning

carcinoma of lung

caregiver

CAT scan, abnormal

CAT scan, emission, abnormal

CD4 counts

central nervous system, infection of

cerebellar atrophy, primary

cerebral death

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cervical spine

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

children

chills

chromosomal abnormality

chromosome 5

climate change

Clinical Pathologic Conference(C.P.C.)

cognition

coma

confusion

congenital heart disease

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

crying, pathologic

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, frontotemporal

dementia, presenile

depression

developmental milestones

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diarrhea

differential diagnosis

diplegia, brachial

disability rating scale, neurological

distal muscle atrophy

distal muscle weakness

encephalitis, central European

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyeloneuritis

encephalopathy

encephalopathy, post anoxic

enterovirus

enterovirus infection of CNS

epidemiology of neurology

ethics in neurology

euthanasia

exercise

facial weakness, bilateral

football neurologic injuries

frontotemporal dementia, behavioral variant

gastrostomy, percutaneous endoscopic

genetic neurologic disorders

genetic screening

genetic testing

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

heralding manifestation

highly active antiretroviral therapy

hospice

human immunodeficiency virus type 1

hunger

hypercapnia

hyperreflexia

hypogammaglobulinemia

hypoxic encephalopathy

immunohistochemistry

immunosuppression

inclusion body myositis

infection

inflexibility, mental

insomnia

intellectual deficit

intermittent positive pressure breathing

internal capsule

intrinsic hand muscles, wasting of

jaw jerk, abnormal

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

laminectomy, cervical

laughing, pathologic

leg atrophy

leg weakness, bilateral

leg weakness, unilateral

leukemia

leukemia, neurologic findings assoc.with

leukoencephalopathy

lid closure, weakness of

life expectancy

life support, withdrawal of

life sustaining treatment

limbic encephalitis

lobar atrophy

locked-in syndrome

medical-legal aspects of neurology

meningismus

mental status, abnormal

Mills syndrome

mimics

minimally conscious state

motor neuron disease, spontaneous recovery

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy

myelitis

myelitis, longitudinal

myelitis, transverse

myelomalacia

myelopathy

myelopathy, ischemic-due to trauma or spondylosis

myeloradiculitis

myocardial infarction

nerve conduction studies

neurologic complications

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic symptoms

neuronal degeneration

neuronopathy

neuronopathy, sensory

neuropathology

neuropathology, brain

neuroprotective agents

next-generation sequencing

nusinersen

old age, neurology of

opiate

owl's eye sign of spinal cord

oxygen therapy

pain

pain, back

pain, increased response

pain, management of chronic

palliative care

paralysis, acute

paralysis, acute areflexic

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

Parkinsonism syndrome

Parkinsonism-dementia complex

patient information and support

persistent vegetative state

personality change

phrenic nerve pacemaker

physician assisted suicide

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poliomyelitis

poliomyelitis-like illness

polymerase chain reaction

positive sharp waves

practice guidelines

pregnancy, neurologic complications in

primary lateral sclerosis

prognosis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

public health

pulmonary embolism

pulmonary function tests

pyramidal tract

pyramidal tract dysfunction

quadriparesis

quality of life

radiculitis

rapidly progressing neurologic illness

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respirator

respiratory arrest

respiratory failure

respiratory tract infection

salivation, excessive

scoliosis

scoliosis, neurologic association with

screening

sedation

sensory symptoms

serologic testing, false negative

single photon emission computed tomography

sleep

sleep pathology and physiology

spinal cord degeneration

spinal cord, compression of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

survival motor neuron gene

syringomyelia

thalamus, lesion of

tick bite

tick-borne encephalitis

tongue, atrophy

tongue, fasciculations of

tracheostomy

trauma

treatment of neurologic disorder

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

West Nile fever

wheelchair

word-finding difficulty

Showing articles 0 to 50 of 8149 Next >>

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Natural History of "Pure" Primary Lateral Sclerosis
Neurol 96:e2231-e2238, Hassan, A.,et al, 2021

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Powassan Virus-A New Reemerging Tick-Borne Disease
Front Public Health 5:342, Fatmi,S.S., et al, 2017

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016

Acute Flaccid Myelitis of Unknown Etiology in California 2012-2015
JAMA 314:2663-2671, Van Haren, K.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Ischemic-Hypoxic Encephalopathy
Adams & Victors Principles of Neurology Chp 40, pg 1133, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
Adams & Victors Principles of Neurology, Chp 39, pg 1118, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Muscle Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Motor Neurone Disease
BMJ 349:g4052, Nageshwaran, S.,et al, 2014

Neurodegenerative causes of death among retired National Football League Players
Neurol 79:1970-1974, Lehman, E.,et al, 2012

Practice Parameter Update: The Care of the Patient with Amyotrophic Lateral Sclerosis: Drug, Nutritional, and Respiratory Therapies (An Evidence-Based Review)
Neurol 73:1218-1226, Miller,R.G.,et al, 2009

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Palliative Care for Patients With Amyotrophic Lateral Sclerosis
JAMA 298:207-216,248, Mitsumoto,H. &Rabkin,J.G., 2007

The Natural History of Primary Lateral Sclerosis
Neurol 66:647-653, Gordon,P.H.,et al, 2006

Clinicopath Conf,Encephalomyelitis Due to West Nile Virus and CLL, Case 22-2005
NEJM 353:287-295, Hollande,H.,et al, 2005

Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
Ann Neurol 54:547-551, Agamanolis,D.P.,et al, 2003

Prognosis in Amyotrophic Lateral Sclerosis
Neurol 60:813-819, del Aguila,M.A.,et al, 2003

Early Symptom Progression Rate is Related to ALS Outcome
Neurol 59:99-103, Chio,A.,et al, 2002

Hospitalization in Amyotrophic Lateral Sclerosis, Causes, Costs, and Outcomes
Neurol 56:753-757, Lechtzin,N.,et al, 2001

Nonpoliovirus Poliomyelitis Simulating Guillain-Barre Syndrome
Arch Neurol 58:1460-1464, Gorson,K.C.&Ropper,A.H., 2001

Reversible ALS-Like Disorder in HIV Infection
Neurol 57:995-1001,945, Moulignier,A.,et al, 2001

Poliomyelitic-Like Illness in Central European Encephalitis
Neurol 55:299-302, Schellinger,P.D. et al, 2000

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

A Prospecitve Study of Preferences and Actual Treatment Choices in ALS
Neurol 53:278-283,248, Albert,S.M.,et al, 1999

Attitudes of Patients with Amyotrophic Lateral Sclerosis and Their Care Givers Toward Assisted Suicide
NEJM 339:967-973,987, Ganzini,L.,et al, 1998

An Analysis of Extended Survival in Patients with Amyotrophic Lateral Sclerosis Treated with Riluzole
Arch Neurol 55:526-528, Riviere,M.,et al, 1998

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
Neurol 48:55-57, Juneja,T.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Palliative Care in Neurology
Neurol 46:870-872, 5981996., Bernat,J.L.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Motor Neuron Disease
JNNP 57:886-896, Leigh,P.N.&Ray-Chaudhuri,K., 1994

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

Showing articles 0 to 50 of 8149 Next >>